L95V (p.Leu95Val) variant of CDH2 (Cadherin-2)
L95V (p.Leu95Val) in CDH2 (Cadherin-2) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Inborn genetic diseases. The record also includes structural context.
L95V (p.Leu95Val) variant details
- p.Leu95Val
- TOPMed rs1354225874
- Uncertain significance
- Inborn genetic diseases
- Missense
- ClinVar: Uncertain significance (Inborn genetic diseases)
- UniProt: Uncertain significance
- Structural context available